Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F287/00—Macromolecular compounds obtained by polymerising monomers on to block polymers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
  • C08F255/02—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having two or three carbon atoms
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
  • C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
  • C08L23/10—Homopolymers or copolymers of propene
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
  • C08L51/06—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond

Definitions

• the invention relates to the use of modified olefin polymers based on modified propylene polymers for producing polyolefin products with simultaneously high requirements for toughness and strength and heat resistance.
• the toughness of products made of propylene polymers can be improved by using polypropylene blends which comprise elastomers, such as polyisobutylene (Martucelli, E., Polymer 24(1983), 1458), ethylene-vinyl acetate copolymers [Thomas, S., Kautschuk-Gummi-Kunstscher (Rubbers and Plastics) 40(1987), 665-671 EPR [Greco, R., Polymer 28(1987), 1929-1936], EPDM [Karger-Kocsis, J., Polymer 23(1982), 699-705] or copolymers made of ethylene and of higher ⁇ -olefins [Yu, T., SPE-ANTEC'94, 2439-2442].
• the disadvantage of these melt blends is a loss of strength and heat resistance with increasing elastomer content.
• the object of the present invention is to provide polyolefin products which satisfy the requirement profile described above and do so using, in order to establish the required mechanical properties, an amount of additives reduced compared with that used in the prior art.
• this object is then achieved by using modified olefin polymers based on modified propylene polymers which olefin polymers have melt indices of from 8 to 100 g/10 min at 230° C./2.16 kp and are obtainable by activating a polyolefin composition comprising
• KM Charpy impact strength at ⁇ 20° C. (kJ/m 2 ) to DIN 53453
• KR Charpy impact strength at +23° C. (kJ/m 2 ) to DIN 53453
• ZM is tensile modulus at 23° C. (MPa) to DIN 53457/ISO 527
• WF is Vicat A softening point (° C.) to ISO 306,
• X 1 from 60 to 70 for the combination of properties KM 1 , KR 1 , ZM 1 , WF 1 ;
• X 2 from 70 to 78 for the combination of properties KM 2 , KR 2 , ZM 2 , WF 2 ,
• mixtures made of semicrystalline propylene polymers and of elastomeric ethylene copolymers in defined mixing ratios which have been modified by reacting with bifunctional monomers in the presence of free-radical generators, are suitable for the polyolefin products with high requirements for toughness, strength and heat resistance.
• bifunctional monomers and “bifunctionally unsaturated monomers” have the same meaning, i.e. monomers having (at least) two double bonds.
• novel polyolefin products are preferably produced using modified olefin polymers prepared by
• the novel polyolefin products are produced from mixtures made of from 85 to 99% by weight of a modified olefin polymer with a melt index of from 8 to 100 g/10 min at 230° C./2.16 kp and from 1 to 15% by weight of an unmodified propylene polymer with a melt index of from 0.5 to 100 g/10 min at 230° C./2.16 kp.
• the unmodified propylene polymers prefferably be formed from propylene homopolymers, from copolymers made of propylene with ⁇ -olefins having from 2 to 18 carbon atoms, preferably from random propylene copolymers, from propylene block copolymers, from random propylene block copolymers and/or from elastomeric polypropylenes, or from mixtures of the polypropylenes mentioned.
• propylene homopolymers which may, if desired, be present in the novel polyolefin products are propylene homopolymers with bimodal molar mass distribution, weight-average molar masses M w of from 500,000 to 1,500,000 g/mol, number-average molar masses M n of from 25,000 to 100,000 g/mol and M w /M n values of from 5 to 60, which were prepared in a reactor cascade using Ziegler-Natta catalysts or metallocene catalysts.
• modified olefin polymers comprise chemically bonded butadiene, isoprene, dimethylbutadiene, divinylbenzene or mixtures of these as bifunctionally unsaturated monomers.
• the average sorption time ⁇ s [s] of the volatile bifunctional monomers on the particulate polyolefin composition is advantageously from 10 to 1000 seconds, preferably from 20 to 800 seconds, particularly preferably from 60 to 600 seconds.
• the sorbed amount of the bifunctionally unsaturated monomers in the modified olefin polymers is preferably from 0.05 to 2% by weight, based on the polyolefin composition used.
• novel polyolefin products are preferably produced by thermoplastic shaping, in particular by extrusion, injection moulding, blow moulding or thermoforming.
• Usual processing temperatures for the polyolefin products produced by extrusion, injection moulding or blow moulding are ranges of temperature from 170 to 300° C.
• blow-moulded polyolefin mouldings are extrusion blow moulding, extrusion stretch blow moulding, injection blow moulding and injection stretch blow moulding (Lee, N., “Plastic blow molding handbook”, Van Norstrand Reinhold Publ. New York 1990; Rosato, D., “Blow molding handbook”, Carl-Hanser-Verlag Kunststoff 1989).
• the injection rate during production of the injection-moulded polyolefin products should be set as high as possible, so that the polyolefin products do not have sink marks or bad flow lines.
• injection moulding machines with injection units which have three-zone screws with a screw length of from 18 to 24 D.
• the polyolefin products which have been produced by extrusion, injection moulding, blow moulding or thermoforming are suitable for use in the packaging industry, in the household equipment industry, in products required in laboratories or in hospitals, in equipment for gardens or agriculture, for transport containers, and also for components in the automotive industry, components of machines and electrical or electronic equipment.
• blow-moulded polyolefin products are bottles, small containers, containers for liquids, liquid-feed parts, air-supply system parts, internal containers, tanks, shock-absorbing components for the automotive industry, folding bellows, protective covers, housings, tubular components, pipes and/or carrying cases.
• injection-moulded polyolefin products are components in the automotive industry, packaging, transport containers, components of machines, of household equipment and of electrical or electronic equipment.
• Particularly preferred polyolefin products are shock-absorbing components of motor vehicles, in particular bumpers, spoilers and side edge protection elements.
• acyl peroxides such as benzoyl peroxide, 4-chlorobenzoyl peroxide, 3-methoxybenzoyl peroxide and/or methylbenzoyl peroxide;
• alkyl peroxides such as allyl tert-butyl peroxide, 2,2-bis(tert-butylperoxybutane), 1,1-bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane, n-butyl 4,4-bis(tert-butylperoxy)valerate, diisopropylaminomethyl tert-amyl peroxide, dimethylaminomethyl tert-amyl peroxide, diethylaminomethyl tert-butyl peroxide, dimethylaminomethyl tert-butyl peroxide, 1,1-di(tert-amylperoxy)cyclohexane, tert-amyl peroxide, tert-butyl cumyl peroxide, tert-butyl peroxide, and/or 1-hydroxybutyl n-butyl peroxide;
• peresters and peroxycarbonates such as butyl peracetate, cumyl peracetate, cumyl perpropionate, cyclohexyl peracetate, di-tert-butyl peradipate, di-tert-butyl perazelate, di-tert-butyl perglutarate, di-tert-butyl perphthalate, di-tert-butyl persebacate, 4-nitrocumyl perpropionate, 1-phenylethyl perbenzoate, phenylethyl nitroperbenzoate, tert-butyl bicyclo[2.2.1]heptanepercarboxylate, tert-butyl 4-carbomethoxyperbutyrate, tert-butyl cyclobutanepercarboxylate, tert-butyl cyclohexylperoxycarboxylate, tert-butyl cyclopentylpercarboxylate, tert-butyl cycl
• Volatile bifunctional monomers which may be used in the preparation of the modified olefin polymers present in the polyolefin products are any bifunctionally unsaturated monomeric compounds which can be sorbed from the gas phase and can be polymerized with the aid of free radicals. Preference is given to the use of the following bifunctionally unsaturated monomers in amounts of from 0.01 to 10% by weight, based on the polyolefin mixture used:
• divinyl compounds such as divinylaniline, m-divinylbenzene, p-divinylbenzene, divinylpentane and/or divinylpropane;
• allyl compounds such as allyl acrylate, allyl methacrylate, allyl methyl maleate and/or allyl vinyl ether;
• dienes such as butadiene, chloroprene, cyclohexadiene, cyclopentadiene, 2,3-dimethylbutadiene, heptadiene, hexadiene, isoprene and/or 1,4-pentadiene;
• Modified olefin polymers preferably present in the polyolefin products are those in which the bifunctionally unsaturated monomer present is chemically bonded butadiene, isoprene, dimethylbutadiene and/or divinylbenzene.
• Continuous gas-solid absorbers used for the sorption of the volatile bifunctional monomers in the preparation of the modified olefin polymers are preferably continuous through-flow mixers.
• the heating and melting of the polyolefin particles within which the bifunctionally unsaturated monomers and the acyl peroxides, alkyl peroxides, hydroperoxides, peresters and/or peroxycarbonates have been sorbed as free-radical generators capable of thermal decomposition takes place in an atmosphere of the volatile bifunctionally unsaturated monomers, preferably in continuous kneaders or extruders, with preference in twin-screw extruders.
• the modified olefin polymers and, respectively, the mixtures made of modified olefin polymers and of unmodified propylene polymers may comprise, as additives, from 0.01 to 2.5% by weight of stabilizers and/or from 0.1 to 1% by weight of antistats and/or from 0.2 to 3% by weight of pigments and/or from 0.05 to 1% by weight of nucleating agents and/or from 1 to 40% by weight of fillers and/or reinforcing materials and/or from 2 to 20% by weight of flame retardants and/or from 0.01 to 1% by weight of processing aids, based on the modified olefin polymers and, respectively, the mixtures made of modified olefin polymers and of unmodified propylene polymers.
• Stabilizers which may be present in the modified olefin polymers or in the mixtures made of modified olefin polymers and of unmodified propylene polymers are preferably mixtures made of from 0.01 to 0.6% by weight of phenolic antioxidants, from 0.01 to 0.6% by weight of free-arylbenzofuranones, from 0.01 to 0.6% by weight of processing stabilizers based on phosphites, from 0.01 to 0.6% by weight of high-temperature stabilizers based on disulphides and on thioethers and/or from 0.01 to 0.8% by weight of sterically hindered amines (HALS).
• HALS sterically hindered amines
• Suitable phenolic antioxidants are 2-tert-butyl-4,6-dimethylphenol, 2,6-di-tert-butyl-4-methylphenol, 2,6-di-tert-butyl-4-isoamylphenol, 2,6-di-tert-butyl-4-ethylphenol, 2-tert-butyl-4,6-diisopropylphenol, 2,6-dicyclopentyl-4-methylphenol, 2,6-di-tert-butyl-4-methoxymethylphenol, 2-tert-butyl-4,6-dioctadecylphenol, 2,5-di-tert-butylhydroquinone, 2,6-di-tert-butyl-4-dihexadecyloxyphenol, 2,2′-methylenebis(6-tert-butyl-4-methylphenol), 4,4′-thiobis(6-tert-butyl-2-methylphenol), octadecy
• a particularly suitable benzofuranone derivative is 5,7-di-tert-butyl-3-(3,4-dimethylphenyl)-3H-benzofuran-2-one.
• HALS compounds are bis-2,2,6,6-tetramethyl-4-piperidyl sebacate and/or poly((6-((1,1,3,3-tetramethylbutyl)amino)-1,3,5-triazine-2,4-diyl)(2, 2,6,6-tetramethyl-4-piperidyl)imino)-1,6-hexanediyl((2,2,6,6-tetramethyl-4-piperidyl)imino))-.
• Nucleating agents which may be present in the modified olefin polymers or in the mixtures made of modified olefin polymers and of unmodified propylene polymers are ⁇ -nucleating agents, such as talc or sodium methylenebis(2,4-di-tert-butylphenyl)phosphate or ⁇ -nucleating agents, such as the dianilide of adipic acid or dibenzoquinacridone or N,N′-dicyclohexyl-2,6-naphthalenedicarboxamide.
• the fillers which may, if desired, be present in the modified olefin polymers or mixtures made of modified olefin polymers and of unmodified propylene polymers are preferably Al 2 O 3 , Al(OH) 3 , barium sulphate, calcium carbonate, glass beads, wood flour, siliceous earth, hollow microbeads, carbon black, talc and/or wollastonite.
• the reinforcers which may, if desired, be present in the modified olefin polymers or mixtures made of modified olefin polymers and of unmodified propylene polymers are preferably aramid fibres, cellulose fibres, flax, jute, kenaf, glass fibres, microfibres made of liquid-crystalline polymers and/or polytetrafluoroethylene fibres.
• Processing aids which may be present in the modified olefin polymers or in the mixtures made of modified olefin polymers and of unmodified propylene polymers are calcium stearate, magnesium stearate and/or waxes.
• novel polyolefin products preferably have gel contents of from 0.5 to 20% by weight.
• a pulverulent polyolefin mixture (melt index 13 g/10 min at 230° C./2.16 kp, average particle diameter 0.55 mm) made of 73% by weight of a propylene homopolymer (melt index 28 g/10 min at 230° C./2.16 kp) and 27% by weight of an ethylene-propylene copolymer (ethylene content 14.3% by weight) is metered continuously into a continuous heatable through-flow mixer. 0.1% by weight of calcium stearate and 0.09% by weight of bis(tert-butylperoxy)-2,5-dimethylhexane, based in each case on the polyolefin mixture, are then metered continuously into the through-flow mixer.
• the polyolefin mixture loaded with free-radical generator capable of thermal decomposition and with auxiliary, is loaded by sorption with 0.92% by weight of divinylbenzene, based on the polyolefin mixture, using a divinylbenzene-nitrogen mixture with a residence time of 6 min at 82° C.
• the pulverulent reaction mixture is transferred to a Berstorff twin-screw extruder (temperature profile 25/160/160/160/165/160/190/220/220/230° C., throughput 5.8 kg/h) and, in contact with the divinylbenzene-nitrogen mixture metered in, and with addition of 0.1% by weight of tetrakis[methylene (3,5-di-tert-butylhydroxyhydrocinnamate)]methane and 0.1% by weight of tris(2,4-di-tert-butylphenyl) phosphite, heated and melted, subjected to preliminary devolatilization with water metered in as entrainer and then to intensive devolatilization, discharged and pelletized.
• a Berstorff twin-screw extruder temperature profile 25/160/160/160/165/160/190/220/220/230° C., throughput 5.8 kg/h
• the resultant modified olefin polymer has a content of bonded divinylbenzene of 0.7% by weight, determined by IR spectroscopy, and a melt index of 14.2 g/10 min at 230° C./2.16 kp.
• the pellets prepared are processed in a Ferromatic Millacron FM 60 injection moulding machine which has a three-zone screw with a screw length of 22 D, at a melt temperature of 225° C. and with a mould temperature of 50° C., according to DIN 16774, to give standard injection-moulded test specimens.
• a pulverulent polyolefin mixture (melt index 0.5 g/10 min at 230° C./2.16 kp, average particle diameter 0.26 mm) made of 75% by weight of a propylene-ethylene copolymer (melt index 0.45 g/10 min at 230° C./2.16 kp, ethylene content 5.5% by weight) and 25% by weight of an ethylene-propylene copolymer (ethylene content 12.5% by weight) is metered continuously into a continuous heatable through-flow mixer. 0.1% by weight of magnesium stearate and 0.25% by weight of tert-butyl peroxyisopropyl carbonate, based in each case on the polyolefin mixture, are then metered continuously into the through-flow mixer.
• the polyolefin mixture loaded with free-radical generator capable of thermal decomposition and with auxiliary, is loaded by sorption with 0.3% by weight of isoprene, based on the polyolefin mixture, using a isoprene-nitrogen mixture with a residence time of 5 min at 76° C.
• the pulverulent reaction mixture is transferred to a Berstorff twin-screw extruder (temperature profile 25/150/155/160/160/160/185/215/220/220° C., throughput 5.2 kg/h) and, in contact with the isoprene-nitrogen mixture metered in, and with addition of 0.1% by weight of 2,2′-methylenebis(6-tert-butyl4-methylphenol) and 0.1% by weight of 5,7-di-tert-butyl-3-(3,4-dimethylphenyl)3H-benzofuran-2-one, heated and melted, subjected to preliminary devolatilization with water metered in as entrainer and then to intensive devolatilization, discharged and pelletized.
• a Berstorff twin-screw extruder temperature profile 25/150/155/160/160/160/185/215/220/220° C., throughput 5.2 kg/h
• the resultant modified olefin polymer has a content of 0.22% by weight of bonded isoprene, determined by IR spectroscopy, and a melt index of 8.2 g/10 min at 230° C./2.16 kp.
• a compound made of 90% by weight of the modified olefin polymer and 10% by weight of an unmodified propylene homopolymer (melt index 28 g/10 min at 230° C./2.16 kp) is extruded through a Brabender laboratory extruder with slot die (temperature profile 85/150/185/220/220/220° C.) to give a rectangular 40 ⁇ 4 mm profile.
• a pulverulent polyolefin mixture (melt index 6 g/10 min at 230° C./2.16 kp, average particle diameter 0.32 mm) made of 65% by weight of a propylene copolymer (melt index 17 g/10 min at 230° C./2.16 kp) and 35% by weight of an ethylene-propylene copolymer (ethylene content 18.2% by weight) is metered continuously into a continuous heatable through-flow mixer. 0.1% by weight of montan wax and 0.18% by weight of methyl benzoyl peroxide, based in each case on the polyolefin mixture, are also metered continuously into the through-flow mixer.
• the polyolefin mixture loaded with free-radical generator capable of thermal decomposition and with auxiliary, is loaded by sorption with 0.45% by weight of butadiene, based on the polyolefin mixture, using a butadiene-nitrogen mixture with a residence time of 4 min at 88° C.
• the pulverulent reaction mixture is transferred to a Berstorff twin-screw extruder (temperature profile 25/150/160/160/165/170/190/220/220/230° C., throughput 6.2 kg/h) and, in contact with the butadiene-nitrogen mixture metered in, and with addition of 0.1% by weight of 2-tert-butyl-4,6-dioctadecylphenol and 0.1% by weight of tris(2,4-di-tert-butylphenyl) phosphite, heated and melted, subjected to preliminary devolatilization with water metered in as entrainer and then to intensive devolatilization, discharged and pelletized.
• a Berstorff twin-screw extruder temperature profile 25/150/160/160/165/170/190/220/220/230° C., throughput 6.2 kg/h
• the resultant modified olefin polymer has a content of bonded butadiene of 0.36% by weight, determined by IR spectroscopy, and a melt index of 14.2 g/10 min at 230° C./2.16 kp.
• the modified olefin polymer (melt index 14.2 g/10 min at 230° C./2.16 kp) is melted using the temperature profile 100/160/205/215/215° C. in the plastifying unit of an injection stretch blow moulding machine comprising plastifying unit with three-zone screw, rotary table with cooled 4-fold injection mould, conditioning mould with three heating zones, blow mould with stretching ram and ejection apparatus, and injected into the 4-fold injection mould, temperature-controlled to 120° C.
• the parison (31 g, wall thickness from 4.5 to 5.5 mm, height 88 mm) is removed from the injection mould by way of the mandrel of the rotary table and introduced into the electrically heated conditioning mould by way of a 90° tipping movement of the rotary table, the heating zones of the conditioning mould having been set at 135° C. (parison base), 138° C. (parison central section) and 135° C. (parison upper section).
• the blow-moulded premoulding is removed and transferred, by way of the mandrel of the rotary table and the 90° tipping movement of the rotary table, into the blow mould, where the blow-moulded premoulding is then subjected to longitudinal stretching by way of the stretching ram and then shaped using compressed air at a pressure of 20 bar.
• the longitudinal stretching ratio for the premoulding in the blow mould is 2.8:1 and the transverse stretching ratio for the premoulding is 2.0:1.
• the blow-moulded container is removed from the opened blow mould after 7.5 s, fed to the ejector by way of a 90° tipping movement of the rotary table, and ejected.
• a pulverulent polyolefin mixture (melt index 8.5 g/10 min at 230° C./2.16 kp, average particle diameter 0.28 mm) made of 82% by weight of a propylene-ethylene copolymer (melt index 14 g/10 min at 230° C./2.16 kp, ethylene content 8.2% by weight) and 18% by weight of an ethylene-propylene copolymer (ethylene content 28.5% by weight) is metered continuously into a continuous heatable through-flow mixer.
• the polyolefin mixture loaded with free-radical generator capable of thermal decomposition and with auxiliary, is loaded by sorption with 0.82% by weight of dimethylbutadiene, based on the polyolefin mixture, using a dimethylbutadiene-nitrogen mixture with a residence time of 5.5 min at 72° C.
• the pulverulent reaction mixture is transferred to a Berstorff twin-screw extruder (temperature profile 25/160/160/160/165/160/190/220/220/230° C., throughput 5.4 kg/h) and, in contact with the dimethylbutadiene-nitrogen mixture metered in, and with addition of 0.15% by weight of 4,4′-thiobis(6-tert-butyl-2-methylphenol) and 0.1% by weight of sodium methylenebis(2,4-di-tert-butylphenol) phosphate, heated and melted, subjected to preliminary devolatilization with water metered in as entrainer and then to intensive devolatilization, discharged and pelletized.
• a Berstorff twin-screw extruder temperature profile 25/160/160/160/165/160/190/220/220/230° C., throughput 5.4 kg/h
• the resultant modified olefin polymer has a content of bonded dimethylbutadiene of 0.70% by weight, determined by IR spectroscopy, and a melt index of 8.2 g/10 min at 230° C./2.16 kp.
• the pellets produced are processed in a Ferromatic Millacron FM 60 injection moulding machine which has a three-zone screw with a screw length of 22 D, at a melt temperature of 225° C. and at a mould temperature of 50° C., in accordance with DIN 16774, to give standard injection moulded test specimens.

Landscapes

• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Graft Or Block Polymers (AREA)
• Compositions Of Macromolecular Compounds (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Applications Claiming Priority (4)

Publications (2)

Family

ID=8169057

Family Applications (1)

Country Status (6)

Cited By (5)

Families Citing this family (4)

Citations (10)

Family Cites Families (2)

• 2000
  • 2000-06-23 EP EP00113359A patent/EP1167404A1/de not_active Withdrawn
• 2001
  • 2001-06-18 AU AU79667/01A patent/AU7966701A/en not_active Abandoned
  • 2001-06-18 US US10/312,472 patent/US6797778B2/en not_active Expired - Lifetime
  • 2001-06-18 BR BRPI0111924-9A patent/BR0111924B1/pt not_active IP Right Cessation
  • 2001-06-18 EP EP01957859A patent/EP1294782B1/de not_active Expired - Lifetime
  • 2001-06-18 WO PCT/EP2001/006842 patent/WO2001098385A1/en active IP Right Grant
  • 2001-06-18 DE DE60125940T patent/DE60125940T2/de not_active Expired - Lifetime

Patent Citations (10)

Non-Patent Citations (7)

Also Published As

Similar Documents

Legal Events